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X–linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene

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Year: 2005
Type: article
Study design: Case Report
Source: Journal of Neurology
DOI: 10.1007/s00415-005-0713-3
Authors: K. Brockmann, A. M. Dumitrescu, Th. T. Best, F. Hanefeld, S. Refetoff
Institutions: Universitätsmedizin Göttingen, University of Göttingen, University of Chicago
Language: English

Topic: Thyroid Disorders and Treatments
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Research Resources
Awards: G1164413914, G3192969681
OpenAlex ID: W2013988137
FWCI: 5.181
Cites: 18
Cited by: 108
Related to: 10
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